CN109662307B - Composite highland barley powder rich in slowly digestible starch and preparation method thereof - Google Patents

Composite highland barley powder rich in slowly digestible starch and preparation method thereof Download PDF

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CN109662307B
CN109662307B CN201811630278.1A CN201811630278A CN109662307B CN 109662307 B CN109662307 B CN 109662307B CN 201811630278 A CN201811630278 A CN 201811630278A CN 109662307 B CN109662307 B CN 109662307B
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highland barley
starch
agaricus bisporus
enzymolysis
slowly digestible
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CN109662307A (en
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王金斌
唐雪明
李文
蒋玮
黄艳娜
宋丽莉
曾海娟
赵琪
刘华
吴潇
吕贝贝
李鹏
武国干
白蓝
陈一帆
孙宇
潘爱虎
贾军伟
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Shanghai Academy of Agricultural Sciences
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    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L29/00Foods or foodstuffs containing additives; Preparation or treatment thereof
    • A23L29/30Foods or foodstuffs containing additives; Preparation or treatment thereof containing carbohydrate syrups; containing sugars; containing sugar alcohols, e.g. xylitol; containing starch hydrolysates, e.g. dextrin
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/125Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives containing carbohydrate syrups; containing sugars; containing sugar alcohols; containing starch hydrolysates
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L7/00Cereal-derived products; Malt products; Preparation or treatment thereof
    • A23L7/10Cereal-derived products
    • A23L7/104Fermentation of farinaceous cereal or cereal material; Addition of enzymes or microorganisms
    • A23L7/107Addition or treatment with enzymes not combined with fermentation with microorganisms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B30/00Preparation of starch, degraded or non-chemically modified starch, amylose, or amylopectin
    • C08B30/04Extraction or purification
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B37/00Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
    • C08B37/0006Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
    • C08B37/0024Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid beta-D-Glucans; (beta-1,3)-D-Glucans, e.g. paramylon, coriolan, sclerotan, pachyman, callose, scleroglucan, schizophyllan, laminaran, lentinan or curdlan; (beta-1,6)-D-Glucans, e.g. pustulan; (beta-1,4)-D-Glucans; (beta-1,3)(beta-1,4)-D-Glucans, e.g. lichenan; Derivatives thereof
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs

Abstract

A composite highland barley powder rich in slowly digestible starch and a preparation method thereof are prepared by taking brown agaricus bisporus and highland barley as raw materials and performing enzymolysis, wherein the composite highland barley powder comprises the following components in percentage by weight: slowly digestible starch 30-56%; 10-40% of fast-digestion starch; 10-40% of digestion-resistant starch. The composite highland barley powder contains rich slowly digestible starch, the slowly digestible starch contains high content of beta-glucan, and can be slowly digested.

Description

Composite highland barley powder rich in slowly digestible starch and preparation method thereof
Technical Field
The invention belongs to the technical field of starch deep processing, and particularly relates to compound highland barley powder rich in slowly digestible starch and a preparation method thereof.
Background
Starch is the main carbohydrate in human diet and can be classified into three categories according to in vitro digestibility and digestion time: rapidly Digestible Starch (RDS), which means starch that can be rapidly digested and absorbed in vivo for 20 min; slowly Digestible Starch (SDS), which is starch that can be completely digested and absorbed in small intestine but has a slow digestion rate, and the digestion time is 20-120 min; resistant Starch (RS), which is starch that is not digested and absorbed in the small intestine of the human body, is only available for microbial fermentation in the large intestine.
The slowly digestible starch has special physiological functions, such as slow absorption, sustained energy release, contribution to maintaining blood sugar steady state, prevention and treatment of various diseases (such as diabetes, glycogen storage disease, cardiovascular and cerebrovascular diseases and the like), therefore, the slowly digestible starch can be applied to development of specific health-care food, heat-sustaining sports drink and other products, and can also be used as a medicament for treating diabetes, cardiovascular and cerebrovascular diseases, obesity and the like, therefore, the improvement of the content of the slowly digestible starch can improve the nutritional value of the starch, and the content of the slowly digestible starch in the existing highland barley powder is 8-9 wt%.
The highland barley (Hordeum Vulgare L. var nudum hook. f.) is a general name for the multi-ridge naked barley in the Qinghai-Tibet plateau area of China, and is also called Yuanmai and Huai wheat in other areas, because the seeds of the highland barley have no shells, the highland barley is also called rice barley or naked barley, is a special type of barley, and belongs to one of varieties of barley of the barley genus of the wheat family of the Gramineae in plant classification.
Agaricus bisporus has effects of reducing blood sugar and cholesterol, and the monosaccharide composition of Agaricus bisporus comprises D-glucose, D-galactose, and D-mannose, and its relative molecular mass is 5.1 × 104~66.0×104Polysaccharides are mainly linked by β -glycosidic bonds. Beta glucan in agaricus bisporus can reduce the content of cholesterol in hypercholesterolemia. The agaricus bisporus has certain effects on hypercholesterolemia and diabetes, and has certain reference value for research and development of medicines for preventing and treating diabetes, atherosclerosis, thrombosis and blood fat reduction.
At present, no report related to the preparation of the slowly digestible starch by the brown agaricus bisporus and the highland barley powder exists.
Disclosure of Invention
The invention aims to provide the compound highland barley powder rich in the slowly digestible starch and the preparation method thereof, the compound highland barley powder contains more than 30% of the slowly digestible starch, can be slowly digested, can maintain satiety for a long time, has high content of beta-glucan in the slowly digestible starch, has the health care characteristics of slow energy release, low blood sugar generation index, high glucose utilization rate and the like, and is easy to realize industrial production.
In order to achieve the purpose, the invention provides the following technical scheme:
the compound highland barley powder rich in slowly digestible starch is prepared by taking brown agaricus bisporus and highland barley as raw materials and performing enzymolysis, and comprises the following components in percentage by weight: 30-56% of slowly digestible starch, 10-40% of quickly digestible starch and 25-40% of digestion-resistant starch.
Preferably, the content of the slowly digestible starch is 40-55%.
Furthermore, the content of the beta-glucan in the composite highland barley powder is 180-210 mg/g.
The invention provides a preparation method of composite highland barley powder rich in slowly digestible starch, which comprises the following steps:
1) gelatinizing
Preparing highland barley powder into highland barley powder milk with the mass concentration of 5-35%, crushing brown agaricus bisporus sporocarp into pulp, and homogenizing to obtain brown agaricus bisporus pulp;
adding brown agaricus bisporus slurry into highland barley milk powder, heating to form paste, and cooling; cooling, adding buffer solution, and adjusting pH to 5.0-6.0 to obtain brown Agaricus bisporus and semen Avenae Nudae powder paste;
wherein, the dosage of the brown agaricus bisporus slurry is 5 to 25 percent of the total volume of the mixed highland barley powder milk and the brown agaricus bisporus slurry;
2) enzymolysis
Carrying out enzymolysis on the cooled brown agaricus bisporus and the highland barley flour paste at the temperature of 40-60 ℃ for 1-5h, and carrying out enzyme inactivation in a boiling water bath to obtain an enzymolysis product;
wherein the enzyme for enzymolysis is alpha-maltogenic amylase and transglucosidase; the addition amount of the alpha-maltogenic amylase is 25-90U/L, and the addition amount of the transglucosidase is 10-45U/L;
3) centrifuging and retrogradation treatment
Subjecting the enzymolysis product to alcohol centrifugation to obtain a precipitate, and refrigerating the precipitate at-20-4 ℃ for 1-9 days to carry out retrogradation treatment to obtain starch gel;
4) drying by baking
And heating and drying the starch gel at the temperature of more than 65 ℃, and crushing to obtain the compound highland barley powder rich in slowly digestible starch.
Preferably, in the step 1), the heating temperature is 90-95 ℃.
Preferably, in the step 2), the buffer solution is sodium acetate water solution, and the molar concentration is 0.5 mol/L.
The invention provides application of the compound highland barley flour rich in slowly digestible starch in food.
The invention adopts an alpha-maltogenic amylase hydrolysis catalysis technology combined with a transglucosidase catalysis technology to produce slowly digestible starch through enzymolysis, and can also generate beta glucan, in particular to a method for producing short molecular chain and multi-branch chain starch molecules (A, B1, B2 and longer chains) by utilizing debranching enzyme alpha-maltogenic amylase, and utilizing transglucosidase to change the property of starch branched chain structure, so that the chain length distribution of the starch is recombined in the enzymolysis process, more new alpha-1, 6 glycosidic bonds are accumulated, the enzymolysis speed is increased at the same time, the aims of removing maltose and breaking the limitation of alpha-1, 6 glycosidic bond proportion are achieved, and the branched chain density and crystal structure are processed by cooperating with starch regeneration, thereby further improving the contents of slowly digestible starch and beta glucan.
In the invention, the addition amount and enzymolysis time of transglucosidase and alpha-maltogenic amylase can directly influence the contents of slowly digested starch and beta-glucan in a final product, and alpha-maltogenic amylase with a certain concentration range not only continuously catalyzes alpha-1, 4 glycosidic bonds, but also catalyzes non-terminal alpha-1, 6 glycosidic bonds of starch to generate D-glucose in a certain time; in the hydrolysis of amylopectin, the α -1, 6-glycosidic bond is a key point for limiting the rate of the hydrolysis reaction. Similarly, a range of transglucosidase concentrations further increases the alpha-1, 6 glycosidic linkages and beta glucan formation over a given time period of enzymatic digestion, increasing the alpha-1, 6 glycosidic linkages in the starch product, and decreasing the rate at which it is enzymatically digested. The invention controls the addition amount of the alpha-maltogenic amylase to be 25-90U/L and the addition amount of the transglucosidase to be 10-45U/L, thereby leading the content (mass percent) of slowly digestible starch in the product to be more than 40 percent in general.
Before enzymolysis, a buffer solution is added into the cooled brown agaricus bisporus and highland barley flour paste, and the pH value is adjusted to be 5.0-6.0, so that the pH value of the brown agaricus bisporus and highland barley flour paste to be subjected to enzymolysis is adjusted to be close to the pH value which is most suitable for performing enzymolysis, alpha-maltogenic amylase and transglucosidase are more favorable for performing enzymolysis, and the yield of slowly digested starch and beta glucan is improved.
The starch retrogradation treatment refers to a physical method for treating starch in a certain temperature range under the condition of excessive or moderate water, and the invention carries out retrogradation treatment on precipitates obtained after centrifugation by refrigerating at-20-4 ℃ for 1-9 days to obtain starch gel, improves dense packing of amorphous areas and reduces crystallinity of crystalline areas, so that the starch has slow digestion characteristics.
The in-vivo digestion process is simulated by adopting an in-vitro digestion method, less than 40 wt% of the compound highland barley powder is digested within the first 20 minutes after being ingested, at least 30% of the compound highland barley powder is digested within 20-120 minutes after being ingested, the compound highland barley powder is slowly digested continuously within 2-4 hours, and the compound highland barley powder is still obviously digested about 6 hours after being ingested.
Compared with the prior art, the invention has the following beneficial effects:
the content of the slowly digestible starch in the composite highland barley powder is 30-56%, the content of the beta-glucan is increased along with the increase of the content of the slowly digestible starch, the content of the beta-glucan in the composite highland barley powder can reach 180-210mg/g, the composite highland barley powder can be slowly digested, satiety is maintained in a long time, at least 60% of the beta-glucan is digested within 2 hours after ingestion, the beta-glucan has continuous slow digestion within 2-4 hours, and the beta-glucan is still obviously digested within about 6 hours after ingestion.
According to the invention, through enzymolysis reaction, the length of an external branch chain of the amylopectin is shortened, the density of the branch chain of the corn starch is increased, and the digestibility of the starch is reduced; the slowly digestible starch is beneficial to slow absorption and sustained energy release, is helpful for maintaining the blood sugar steady state, and can be used for preventing and treating various diseases (such as diabetes, glycogen storage disease, cardiovascular and cerebrovascular diseases, etc.); beta-glucan as an immunomodulator can trigger a series of effects, so that the human immune system is more efficient.
The food prepared from the composite highland barley flour product has long retention time in intestines and stomach, promotes the sufficient peristalsis of the intestines, can maintain satiety for a long time, and has the characteristics of sustained energy release, low glycemic index and high glucose utilization rate.
Drawings
FIG. 1 is a molecular mass distribution chart of the mixed brown agaricus bisporus and highland barley flour raw materials.
FIG. 2 is the molecular mass distribution chart of the composite highland barley flour product obtained in example 1 of the present invention.
FIG. 3 is a graph showing the results of in vitro digestion experiments for seven biscuits according to example 6 of the invention.
FIG. 4 shows a biscuit made of the composite highland barley flour of the invention.
Detailed Description
The invention is further illustrated by the following examples and figures.
Example 1
Preparing highland barley powder milk with highland barley powder raw material mass concentration of 5%, crushing fresh brown agaricus bisporus fruit bodies into pulp, homogenizing, adding the brown agaricus bisporus pulp into the highland barley powder milk, and heating at 90 ℃ to form brown agaricus bisporus and highland barley powder paste; wherein the brown agaricus bisporus slurry accounts for 5% of the total volume of the mixture.
After cooling, 0.5mol/L sodium acetate buffer was added to adjust the pH to 5.0.
And performing enzymolysis on the cooled brown agaricus bisporus and the highland barley flour paste at 40 ℃, wherein the addition amount of enzyme for enzymolysis, including alpha-maltogenic amylase, is 25U/L, the addition amount of transglucosidase is 10U/L, performing enzyme inactivation in a boiling water bath to obtain an enzymolysis product, wherein the enzymolysis time is 1h, and performing enzyme inactivation in the boiling water bath for 5 min.
And then cooling the starch milk, adding 2 times of volume of absolute ethyl alcohol, precipitating macromolecular brown agaricus bisporus and highland barley powder dextrin, standing, and centrifuging at 3000r/min for 10min to obtain starch gel.
And (4) refrigerating the starch gel obtained by centrifugation at-20 ℃ for 5 days, drying and grinding to obtain the powdery starch sample composite highland barley powder.
In the composite highland barley powder, the content of slowly digestible starch is 49.87 wt%, the content of rapidly digestible starch is 14.32 wt%, the content of digestion resistant starch is 32.82 wt%, and the content of beta glucan is 184.38 mg/g.
Example 2
Preparing highland barley powder milk with the highland barley powder raw material mass concentration of 35%, crushing fresh brown agaricus bisporus fruit bodies into pulp, homogenizing, adding the brown agaricus bisporus pulp into the highland barley powder milk, and heating at 95 ℃ to form brown agaricus bisporus and highland barley powder paste; wherein the brown agaricus bisporus slurry accounts for 25% of the total volume of the mixture.
Cooling, adding 0.5mol/L sodium acetate buffer solution, and adjusting the pH value to 6.0; and performing enzymolysis on the cooled brown agaricus bisporus and the highland barley flour paste at the temperature of 60 ℃, wherein the addition amount of enzyme for enzymolysis, including alpha-maltogenic amylase, is 90U/L, the addition amount of transglucosidase is 45U/L, performing enzyme inactivation in a boiling water bath to obtain an enzymolysis product, the enzymolysis time is 5h, and performing enzyme inactivation in the boiling water bath for 5 min.
Then, cooling the starch milk, adding 2 times of volume of absolute ethyl alcohol, precipitating macromolecular brown agaricus bisporus and highland barley powder dextrin, standing, and centrifuging at 3000r/min for 10min to obtain starch gel.
And (3) refrigerating the starch gel obtained by centrifugation at 4 ℃ for 5 days, drying and grinding to obtain the powdered starch sample composite highland barley powder, wherein the content of slowly digestible starch is 44.75 wt%, the content of rapidly digestible starch is 15.31 wt%, the content of digestion resistant starch is 38.19 wt%, and the content of beta glucan is 189.12 mg/g.
Example 3
Preparing highland barley powder milk with highland barley powder raw material mass concentration of 20%, crushing fresh brown agaricus bisporus fruit bodies into pulp, homogenizing, adding the brown agaricus bisporus pulp into the highland barley powder milk, and heating at 93 ℃ to form brown agaricus bisporus and highland barley powder paste; wherein the brown agaricus bisporus slurry accounts for 15 percent of the total volume of the mixture.
Cooling, adding 0.5mol/L sodium acetate buffer solution, and adjusting the pH value to 5.5; and performing enzymolysis on the cooled brown agaricus bisporus and the highland barley flour paste at the temperature of 50 ℃, wherein the addition amount of enzymes for enzymolysis, including alpha-maltogenic amylase, is 75U/L, the addition amount of transglucosidase is 35U/L, performing enzyme inactivation in a boiling water bath to obtain an enzymolysis product, wherein the enzymolysis time is 3h, and performing enzyme inactivation in the boiling water bath for 5 min.
Then, cooling the starch milk, adding 2 times of volume of absolute ethyl alcohol, precipitating macromolecular brown agaricus bisporus and highland barley powder dextrin, standing, and centrifuging at 3000r/min for 10min to obtain starch gel.
And (3) refrigerating the starch gel obtained by centrifugation at-5 ℃ for 5 days, drying and grinding to obtain the powdered starch sample composite highland barley powder, wherein the content of slowly digestible starch is 55.46 wt%, the content of rapidly digestible starch is 11.94 wt%, the content of digestion resistant starch is 29.54 wt%, and the content of beta glucan is 205.82 mg/g.
Example 4
Weighing a mixed sample of brown agaricus bisporus and highland barley powder raw materials, and dissolving 5mg of each of the compound highland barley powder products obtained in the embodiment 1 in 1ml of a mixture containing 0.15mol/L of NaNO3And 0.05mol/L NaH2PO4(pH 7), heating and stirring at 90 deg.C for 2h, stirring at room temperature for 12h, centrifuging at 12000r/min for 20min, collecting supernatant, filtering with 0.45 μm nylon microporous membrane, and performing HPSEC-MALLS-RI analysis, wherein the analysis results are shown in FIG. 1 and FIG. 2, wherein the abscissa represents the elution time, and the smaller the molecular weight of the starch, the longer the elution time. The ordinate MV is the standard signal output by the instrument and represents the amount of starch, i.e. the higher the peak is, the more starch of this certain molecular weight is.
As shown in FIG. 1, in the mixed sample of original brown Agaricus bisporus and semen Avenae Nudae powder, the peak molecular weight of amylopectin is 1.1 × 107The peak area is a large proportion; the peak molecular weight of amylose is 2.3X 105The original brown agaricus bisporus and the highland barley powder contain a large amount of amylopectin with larger molecular weight and amylose with smaller molecular weight.
As shown in FIG. 2, in the composite highland barley flour product of example 1 of the present invention, the distribution of starch molecular weight is significantly changed, wherein the peak MW of amylopectin is 7.7 × 105Amylose having a peak MW of 1.8X 103Therefore, the area of the amylopectin peak in the brown agaricus bisporus and highland barley powder products is reduced, and the proportion of starch molecules with low molecular weight is increased.
Example 5
In-vitro digestion determination is carried out on seven biscuit samples, namely, a mixed raw material of brown agaricus bisporus and highland barley flour, a compound highland barley flour product rich in slowly digestible starch obtained in example 1, a biscuit prepared from common corn starch and wheat starch, a coarse cereal biscuit, an oat biscuit, a calcium milk biscuit and the like purchased in the market, seven time points, namely 0min, 30min, 60min, 90min, 120min, 150min and 180min are selected to determine the glucose content in the hydrolysate, and the content of the slowly digestible starch of various products is calculated to obtain digestion data.
Adopting an improved in-vitro simulated digestion method: weighing 400mg of a sample to be detected, adding 5mL of water, mixing uniformly, oscillating in a water bath kettle at 95 ℃ for 20min, cooling to room temperature, putting in a constant-temperature water bath kettle at 37 ℃ until the temperature rises to 37 ℃, adding sodium acetate buffer solution (pH 5.2) to fix the volume to 15mL, adding 5mL of mixed enzyme solution of 300U/mL pancreatic alpha-amylase and 40U/mL saccharifying enzyme, and oscillating, digesting and hydrolyzing at 37 ℃. Hydrolyzing for 20min and 120min, respectively taking out 0.5mL of hydrolysate, adding 20mL of 66% ethanol into a centrifuge tube, standing, centrifuging, taking 1mL of centrifuged supernatant, and determining the content of glucose by using a 3, 5-dinitrosalicylic acid method to obtain the condition of determining the content of slowly digested starch.
The method for measuring the glucose content by adopting a 3, 5-dinitrosalicylic acid (DNS) method comprises the following specific steps:
(1) preparation of DNS reagent
Weighing 262mL of NaOH solution (2mol/L), sequentially adding 6.3g of 3, 5-dinitrosalicylic acid and 500mL of 27% potassium sodium tartrate, uniformly mixing, adding 5g of phenol and 5g of anhydrous sodium sulfite, fully stirring, cooling at room temperature, finally fixing the volume to 1000mL, placing in a brown reagent bottle, keeping in the dark, and placing in a refrigerator for one week for use.
(2) Standard curve for glucose
8 standard solutions are prepared, glucose solution, distilled water and DNS reagent are prepared according to the proportion of Table 1, the serial numbers are 1, 2, 3, 4, 5, 6, 7 and 8 in sequence, and the solution concentrations are 0.2mg/ml, 0.4mg/ml, 0.6mg/ml, 0.8mg/ml, 1.0mg/ml, 1.2mg/ml, 1.4mg/ml and 1.6mg/ml in sequence.
Using the blank solution as a comparison, heating each sample solution in boiling water bath for 5min, immediately cooling in ice bath for 10min, adding 21.5ml of distilled water, and measuring the optical density D of the 8 standard solutions540See Table 1, optical Density D540Measuring for 3 times, taking an average value, drawing a standard curve by taking the glucose concentration as an abscissa and the optical density value as an ordinate, and obtaining a standard curve equation: y is 0.466X-0.0158R2=0.9969。
TABLE 1
Optical density Blank space 1 2 3 4 5 6 7 8
D 540 0 0.0644 0.1710 0.2494 0.3449 0.4724 0.5452 0.6495 0.7162
(3) Determination of sugar content in supernatant
Collecting supernatant 1ml after digestion for 20min and 120min, respectively, adding 1ml distilled water and DNS reagent 1.5ml, heating in boiling water bath for 5min, immediately ice-cooling for 10min, adding 21.5ml distilled water, and measuring absorbance with blank solution as control to obtain optical density D540Average value.
Optical density D540Substituting the average value into a standard curve equation: and Y is 0.466X-0.0158, the content of glucose in the supernatant after 20min and 120min is calculated, and the calculation formula of the SDS content is as follows:
SDS(%)=(m120-m20)×100%/mTS
in the formula: m is20The glucose mass/mg after 20min of hydrolysis; m is120Glucose mass/mg after 120min of hydrolysis; m isTSIs the total starch mass/mg in the sample.
HPSEC-MALLS-RI analysis: series connection of a TSK-GE-G6000PWX gel chromatographic column and a G3000PWXL gel chromatographic column is adopted, the sample injection amount is 100 mu L, the mobile phase is a mixed solution of NaNO3(0.15mol/L) and NaH2PO4(0.05mol/L), the flow rate is 0.5ml/min, and the temperature of the chromatographic column is kept at 35 ℃ by using a column incubator; helium and neon are used as light source gas of MALLS, and the wavelength is selected from 623.8 nm. The refractive index increment (dn/dc) of starch in solution was calculated as 0.146 mL/g.
Fig. 3 is a result of in vitro digestion determination of different biscuits, and fig. 3 shows that the biscuit prepared by using the composite highland barley flour obtained in example 1 of the present invention has a glucose concentration increase tendency lower than that of other six biscuits, the glucose concentration continuously and slowly increases within 30-120 min, and the glucose concentration increase range within 0-30 min is also lower than that of other six biscuits, which indicates that the starch digestion rate can be effectively improved by adding the composite highland barley flour product (fig. 4) rich in slowly digestible starch of the present invention, and satiety can be maintained for a longer time.
The compound highland barley powder of the invention has less than 40 wt% of the compound highland barley powder digested within the first 20 minutes after ingestion, and at least 30% of the compound highland barley powder is digested within 20-120 minutes after ingestion, is slowly digested continuously within 2-4 hours, and is still obviously digested about 6 hours after ingestion.

Claims (7)

1. The compound highland barley powder rich in slowly digestible starch is prepared by taking brown agaricus bisporus and highland barley as raw materials and performing enzymolysis, and comprises the following components in percentage by weight: 30-56% of slowly digestible starch, 10-40% of quickly digestible starch and 25-40% of digestion-resistant starch;
the composite highland barley powder is prepared by the following steps:
1) gelatinizing
Preparing highland barley powder into highland barley powder milk with the mass concentration of 5-35%, crushing brown agaricus bisporus sporocarp into pulp, and homogenizing to obtain brown agaricus bisporus pulp;
adding brown agaricus bisporus slurry into highland barley milk powder, heating to form paste, and cooling; cooling, adding buffer solution, and adjusting pH to 5.0-6.0 to obtain brown Agaricus bisporus and semen Avenae Nudae powder paste;
wherein, the dosage of the brown agaricus bisporus slurry is 5 to 25 percent of the total volume of the mixed highland barley powder milk and the brown agaricus bisporus slurry;
2) enzymolysis
Carrying out enzymolysis on the cooled brown agaricus bisporus and the highland barley flour paste at the temperature of 40-60 ℃ for 1-5h, and carrying out enzyme inactivation in a boiling water bath to obtain an enzymolysis product;
wherein the enzyme for enzymolysis is alpha-maltogenic amylase and transglucosidase; the addition amount of the alpha-maltogenic amylase is 25-90U/L, and the addition amount of the transglucosidase is 10-45U/L;
3) centrifuging and retrogradation treatment
Subjecting the enzymolysis product to alcohol centrifugation to obtain a precipitate, and refrigerating the precipitate at-20-4 ℃ for 1-9 days to carry out retrogradation treatment to obtain starch gel;
4) drying by baking
And heating and drying the starch gel at the temperature of more than 65 ℃, and crushing to obtain the compound highland barley powder rich in slowly digestible starch.
2. The compound highland barley flour rich in slowly digestible starch as claimed in claim 1, wherein the slowly digestible starch is 40-55%.
3. The highland barley flour rich in slowly digestible starch as claimed in claim 1 or 2, wherein the content of β -glucan in the highland barley flour is 180-210 mg/g.
4. The method for preparing the compound highland barley flour rich in slowly digestible starch as claimed in claim 1, comprises the following steps:
1) gelatinizing
Preparing highland barley powder into highland barley powder milk with the mass concentration of 5-35%, crushing brown agaricus bisporus sporocarp into pulp, and homogenizing to obtain brown agaricus bisporus pulp;
adding brown agaricus bisporus slurry into highland barley milk powder, heating to form paste, and cooling; cooling, adding buffer solution, and adjusting pH to 5.0-6.0 to obtain brown Agaricus bisporus and semen Avenae Nudae powder paste;
wherein, the dosage of the brown agaricus bisporus slurry is 5 to 25 percent of the total volume of the mixed highland barley powder milk and the brown agaricus bisporus slurry;
2) enzymolysis
Carrying out enzymolysis on the cooled brown agaricus bisporus and the highland barley flour paste at the temperature of 40-60 ℃ for 1-5h, and carrying out enzyme inactivation in a boiling water bath to obtain an enzymolysis product;
wherein the enzyme for enzymolysis is alpha-maltogenic amylase and transglucosidase; the addition amount of the alpha-maltogenic amylase is 25-90U/L, and the addition amount of the transglucosidase is 10-45U/L;
3) centrifuging and retrogradation treatment
Subjecting the enzymolysis product to alcohol centrifugation to obtain a precipitate, and refrigerating the precipitate at-20-4 ℃ for 1-9 days to carry out retrogradation treatment to obtain starch gel;
4) drying by baking
And heating and drying the starch gel at the temperature of more than 65 ℃, and crushing to obtain the compound highland barley powder rich in slowly digestible starch.
5. The method for preparing the composite highland barley flour as claimed in claim 4, wherein the heating temperature in the step 1) is 90-95 ℃.
6. The method for preparing the composite highland barley flour as claimed in claim 4, wherein in the step 2), the buffer solution is sodium acetate aqueous solution, phosphoric acid aqueous solution or citric acid aqueous solution.
7. Use of the compound highland barley flour rich in slowly digestible starch as claimed in claim 1 or 2 in food.
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